Pelvalon, Inc. is one of 17602 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pelvalon, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Eclipse System
1
Total
1
Cleared
0
Denied
Pelvalon, Inc. has 1 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Pelvalon, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Domecus Consulting Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Pelvalon, Inc.
1 devices